College of Life Sciences and Key Laboratory of Bioactive Materials Ministry of Education, Nankai University, 300071 Tianjin, PR China.
School of Medicine, State Key Laboratory of Medicinal Chemical Biology, Nankai University, 300071 Tianjin, PR China.
Brain Res Bull. 2020 Aug;161:166-176. doi: 10.1016/j.brainresbull.2020.05.007. Epub 2020 May 28.
Tacrine (Amino tetrahydroacridine hydrochloride hydrate) is a non-competitive and reversible inhibitor of acetylcholine esterase, and butylcholinesterase. Alzheimer's disease (AD) shows multiple types of pathological pathway in which cholinergic neuron deficiency is 95 % popular and the oldest pathological mechanism. However, the effect of tacrine on the hippocampal dependent memory is not yet known. In this study, we did verify that tacrine induced recovery of the specific pattern associated memory along with long-term memory through the improvement in the pattern of neural oscillation from deficits condition in the hippocampus of 6th month old AD mice. Our results showed that tacrine improved the performance of Morris water maze related spatial cognitive functions, and enhanced LTP in AD-TAC mice. Furthermore, our results implied that tacrine strongly improve the patterns of neural oscillations, and hippocampal synaptic plasticity in the 6th month old APP-PS1 double transgenic AD-TAC mice via changing the theta and alpha power spectra including with the improvement in theta, alpha and gamma synchronization. Moreover, tacrine generated the improvement in the theta cross spectra, theta-gamma phase-phase synchronization and theta-gamma phase-amplitude coupling. Besides, the data represented that tacrine accelerated the expression of NR2B, SYP and GAD65 while it caused deceleration on the expression of GAD67 neurotransmitter and Aβ. Thus, our results infer that tacrine works as a strong causative agent for improving the specific pattern-associated spatial long-term memory in the AD mice without showing any side effect.
他克林(盐酸氨基四氢吖啶水合物)是非竞争性和可逆的乙酰胆碱酯酶和丁酰胆碱酯酶抑制剂。阿尔茨海默病(AD)显示出多种病理途径,其中胆碱能神经元缺乏占 95%,是最古老的病理机制。然而,他克林对海马依赖记忆的影响尚不清楚。在这项研究中,我们通过改善 6 个月大 AD 小鼠海马中的神经振荡模式,证实他克林诱导与特定模式相关的记忆恢复以及长时记忆,从而导致特定模式相关记忆的恢复。我们的结果表明,他克林改善了 Morris 水迷宫相关的空间认知功能,并增强了 AD-TAC 小鼠的 LTP。此外,我们的结果表明,他克林通过改变θ和α功率谱,包括改善θ、α和γ同步,强烈改善了 6 个月大的 APP-PS1 双转基因 AD-TAC 小鼠的神经振荡模式和海马突触可塑性。此外,他克林产生了θ交叉谱、θ-γ相位-相位同步和θ-γ相位-幅度耦合的改善。此外,数据表明,他克林加速了 NR2B、SYP 和 GAD65 的表达,同时减缓了神经递质 GAD67 和 Aβ的表达。因此,我们的结果推断他克林作为一种强大的促发剂,可改善 AD 小鼠的特定模式相关空间长时记忆,而没有显示任何副作用。